Back to Multiple platform build/check report for BioC 3.20:   simplified   long
ABCDE[F]GHIJKLMNOPQRSTUVWXYZ

This page was generated on 2024-12-23 12:06 -0500 (Mon, 23 Dec 2024).

HostnameOSArch (*)R versionInstalled pkgs
nebbiolo2Linux (Ubuntu 24.04.1 LTS)x86_644.4.2 (2024-10-31) -- "Pile of Leaves" 4744
palomino8Windows Server 2022 Datacenterx644.4.2 (2024-10-31 ucrt) -- "Pile of Leaves" 4487
merida1macOS 12.7.5 Montereyx86_644.4.2 (2024-10-31) -- "Pile of Leaves" 4515
kjohnson1macOS 13.6.6 Venturaarm644.4.2 (2024-10-31) -- "Pile of Leaves" 4467
Click on any hostname to see more info about the system (e.g. compilers)      (*) as reported by 'uname -p', except on Windows and Mac OS X

Package 716/2289HostnameOS / ArchINSTALLBUILDCHECKBUILD BIN
FindIT2 1.12.0  (landing page)
Guandong Shang
Snapshot Date: 2024-12-19 13:00 -0500 (Thu, 19 Dec 2024)
git_url: https://git.bioconductor.org/packages/FindIT2
git_branch: RELEASE_3_20
git_last_commit: 1bcb4fc
git_last_commit_date: 2024-10-29 11:01:40 -0500 (Tue, 29 Oct 2024)
nebbiolo2Linux (Ubuntu 24.04.1 LTS) / x86_64  OK    OK    OK  UNNEEDED, same version is already published
palomino8Windows Server 2022 Datacenter / x64  OK    OK    OK    OK  UNNEEDED, same version is already published
merida1macOS 12.7.5 Monterey / x86_64  OK    OK    OK    OK  UNNEEDED, same version is already published
kjohnson1macOS 13.6.6 Ventura / arm64  OK    OK    OK    OK  UNNEEDED, same version is already published


CHECK results for FindIT2 on merida1

To the developers/maintainers of the FindIT2 package:
- Allow up to 24 hours (and sometimes 48 hours) for your latest push to git@git.bioconductor.org:packages/FindIT2.git to reflect on this report. See Troubleshooting Build Report for more information.
- Use the following Renviron settings to reproduce errors and warnings.
- If 'R CMD check' started to fail recently on the Linux builder(s) over a missing dependency, add the missing dependency to 'Suggests:' in your DESCRIPTION file. See Renviron.bioc for more information.

raw results


Summary

Package: FindIT2
Version: 1.12.0
Command: /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings FindIT2_1.12.0.tar.gz
StartedAt: 2024-12-20 03:26:14 -0500 (Fri, 20 Dec 2024)
EndedAt: 2024-12-20 03:38:26 -0500 (Fri, 20 Dec 2024)
EllapsedTime: 732.1 seconds
RetCode: 0
Status:   OK  
CheckDir: FindIT2.Rcheck
Warnings: 0

Command output

##############################################################################
##############################################################################
###
### Running command:
###
###   /Library/Frameworks/R.framework/Resources/bin/R CMD check --install=check:FindIT2.install-out.txt --library=/Library/Frameworks/R.framework/Resources/library --no-vignettes --timings FindIT2_1.12.0.tar.gz
###
##############################################################################
##############################################################################


* using log directory ‘/Users/biocbuild/bbs-3.20-bioc/meat/FindIT2.Rcheck’
* using R version 4.4.2 (2024-10-31)
* using platform: x86_64-apple-darwin20
* R was compiled by
    Apple clang version 14.0.0 (clang-1400.0.29.202)
    GNU Fortran (GCC) 12.2.0
* running under: macOS Monterey 12.7.6
* using session charset: UTF-8
* using option ‘--no-vignettes’
* checking for file ‘FindIT2/DESCRIPTION’ ... OK
* this is package ‘FindIT2’ version ‘1.12.0’
* package encoding: UTF-8
* checking package namespace information ... OK
* checking package dependencies ... OK
* checking if this is a source package ... OK
* checking if there is a namespace ... OK
* checking for hidden files and directories ... OK
* checking for portable file names ... OK
* checking for sufficient/correct file permissions ... OK
* checking whether package ‘FindIT2’ can be installed ... OK
* checking installed package size ... OK
* checking package directory ... OK
* checking ‘build’ directory ... OK
* checking DESCRIPTION meta-information ... OK
* checking top-level files ... OK
* checking for left-over files ... OK
* checking index information ... OK
* checking package subdirectories ... OK
* checking code files for non-ASCII characters ... OK
* checking R files for syntax errors ... OK
* checking whether the package can be loaded ... OK
* checking whether the package can be loaded with stated dependencies ... OK
* checking whether the package can be unloaded cleanly ... OK
* checking whether the namespace can be loaded with stated dependencies ... OK
* checking whether the namespace can be unloaded cleanly ... OK
* checking dependencies in R code ... OK
* checking S3 generic/method consistency ... OK
* checking replacement functions ... OK
* checking foreign function calls ... OK
* checking R code for possible problems ... OK
* checking Rd files ... OK
* checking Rd metadata ... OK
* checking Rd cross-references ... OK
* checking for missing documentation entries ... OK
* checking for code/documentation mismatches ... OK
* checking Rd \usage sections ... OK
* checking Rd contents ... OK
* checking for unstated dependencies in examples ... OK
* checking contents of ‘data’ directory ... OK
* checking data for non-ASCII characters ... OK
* checking data for ASCII and uncompressed saves ... OK
* checking files in ‘vignettes’ ... OK
* checking examples ... OK
Examples with CPU (user + system) or elapsed time > 5s
                      user system elapsed
findIT_regionRP     11.780  0.160  12.262
calcRP_region       10.931  0.178  11.670
calcRP_TFHit         6.609  0.312   7.529
plot_peakGeneCor     6.830  0.080   7.011
peakGeneCor          6.574  0.245   7.165
calcRP_coverage      5.793  0.562   7.175
enhancerPromoterCor  5.430  0.089   5.959
* checking for unstated dependencies in ‘tests’ ... OK
* checking tests ...
  Running ‘testthat.R’
 OK
* checking for unstated dependencies in vignettes ... OK
* checking package vignettes ... OK
* checking running R code from vignettes ... SKIPPED
* checking re-building of vignette outputs ... SKIPPED
* checking PDF version of manual ... OK
* DONE

Status: OK


Installation output

FindIT2.Rcheck/00install.out

##############################################################################
##############################################################################
###
### Running command:
###
###   /Library/Frameworks/R.framework/Resources/bin/R CMD INSTALL FindIT2
###
##############################################################################
##############################################################################


* installing to library ‘/Library/Frameworks/R.framework/Versions/4.4-x86_64/Resources/library’
* installing *source* package ‘FindIT2’ ...
** using staged installation
** R
** data
** inst
** byte-compile and prepare package for lazy loading
** help
*** installing help indices
** building package indices
** installing vignettes
** testing if installed package can be loaded from temporary location
** testing if installed package can be loaded from final location
** testing if installed package keeps a record of temporary installation path
* DONE (FindIT2)

Tests output

FindIT2.Rcheck/tests/testthat.Rout


R version 4.4.2 (2024-10-31) -- "Pile of Leaves"
Copyright (C) 2024 The R Foundation for Statistical Computing
Platform: x86_64-apple-darwin20

R is free software and comes with ABSOLUTELY NO WARRANTY.
You are welcome to redistribute it under certain conditions.
Type 'license()' or 'licence()' for distribution details.

R is a collaborative project with many contributors.
Type 'contributors()' for more information and
'citation()' on how to cite R or R packages in publications.

Type 'demo()' for some demos, 'help()' for on-line help, or
'help.start()' for an HTML browser interface to help.
Type 'q()' to quit R.

> library(testthat)
> library(FindIT2)
Loading required package: GenomicRanges
Loading required package: stats4
Loading required package: BiocGenerics

Attaching package: 'BiocGenerics'

The following objects are masked from 'package:stats':

    IQR, mad, sd, var, xtabs

The following objects are masked from 'package:base':

    Filter, Find, Map, Position, Reduce, anyDuplicated, aperm, append,
    as.data.frame, basename, cbind, colnames, dirname, do.call,
    duplicated, eval, evalq, get, grep, grepl, intersect, is.unsorted,
    lapply, mapply, match, mget, order, paste, pmax, pmax.int, pmin,
    pmin.int, rank, rbind, rownames, sapply, saveRDS, setdiff, table,
    tapply, union, unique, unsplit, which.max, which.min

Loading required package: S4Vectors

Attaching package: 'S4Vectors'

The following object is masked from 'package:utils':

    findMatches

The following objects are masked from 'package:base':

    I, expand.grid, unname

Loading required package: IRanges
Loading required package: GenomeInfoDb
> if (!requireNamespace("TxDb.Athaliana.BioMart.plantsmart28")) {
+     stop("unable to load TxDb.Athaliana.BioMart.plantsmart28")
+ }
Loading required namespace: TxDb.Athaliana.BioMart.plantsmart28
> 
> test_check("FindIT2")
>> preparing gene features information...		2024-12-20 03:36:18
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:36:20
>> preparing weight info...		2024-12-20 03:36:21
>> loading E50h_sampleChr5.bw info...		2024-12-20 03:36:21
------------
>> extracting and calcluating Chr5 signal...		2024-12-20 03:36:21
>> dealing with Chr5 left gene signal...		2024-12-20 03:36:26
>> norming Chr5RP accoring to the whole Chr RP...		2024-12-20 03:36:27
>> merging all Chr RP together...		2024-12-20 03:36:27
>> done		2024-12-20 03:36:27
>> checking seqlevels match...		2024-12-20 03:36:27
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2024-12-20 03:36:27
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:36:29
>> finding overlap peak in gene scan region...		2024-12-20 03:36:29
>> dealing with left peak not your gene scan region...		2024-12-20 03:36:29
>> merging two set peaks...		2024-12-20 03:36:30
>> calculating distance and dealing with gene strand...		2024-12-20 03:36:30
>> merging all info together ...		2024-12-20 03:36:30
>> done		2024-12-20 03:36:30
>> calculating peakCenter to TSS using peak-gene pair...		2024-12-20 03:36:30
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2024-12-20 03:36:32
>> calculating RP using centerToTSS and peak score2024-12-20 03:36:32
>> merging all info together		2024-12-20 03:36:37
>> done		2024-12-20 03:36:38
>> calculating peakCenter to TSS using peak-gene pair...		2024-12-20 03:36:39
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2024-12-20 03:36:40
>> calculating RP using centerToTSS and peak score2024-12-20 03:36:40
>> merging all info together		2024-12-20 03:36:46
>> done		2024-12-20 03:36:47
>> checking seqlevels match...		2024-12-20 03:36:48
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2024-12-20 03:36:48
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:36:49
>> finding overlap peak in gene scan region...		2024-12-20 03:36:49
>> dealing with left peak not your gene scan region...		2024-12-20 03:36:49
>> merging two set peaks...		2024-12-20 03:36:50
>> calculating distance and dealing with gene strand...		2024-12-20 03:36:50
>> merging all info together ...		2024-12-20 03:36:50
>> done		2024-12-20 03:36:50
>> calculating peakCenter to TSS using peak-gene pair...		2024-12-20 03:36:50
>> calculating RP using centerToTSS and TF hit		2024-12-20 03:36:52
>> merging all info together		2024-12-20 03:36:52
>> done		2024-12-20 03:36:52
>> calculating peakCenter to TSS using peak-gene pair...		2024-12-20 03:36:52
>> calculating RP using centerToTSS and TF hit		2024-12-20 03:36:54
>> merging all info together		2024-12-20 03:36:54
>> done		2024-12-20 03:36:54
>> checking seqlevels match...		2024-12-20 03:36:56
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2024-12-20 03:36:56
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:36:58
>> finding overlap peak in gene scan region...		2024-12-20 03:36:58
>> dealing with left peak not your gene scan region...		2024-12-20 03:36:58
>> merging two set peaks...		2024-12-20 03:36:58
>> calculating distance and dealing with gene strand...		2024-12-20 03:36:58
>> merging all info together ...		2024-12-20 03:36:58
>> done		2024-12-20 03:36:58
>> calculating peakCenter to TSS using peak-gene pair...		2024-12-20 03:36:58
>> pre-filling 1356 noAssoc peak gene's RP with 0...		2024-12-20 03:37:00
>> calculating RP using centerToTSS and peak score2024-12-20 03:37:00
>> merging all info together		2024-12-20 03:37:04
>> done		2024-12-20 03:37:05
>> extracting RP info from regionRP...		2024-12-20 03:37:06
>> dealing with TF_GR_databse...		2024-12-20 03:37:07
>> calculating percent and p-value...		2024-12-20 03:37:07
>> dealing withE5_0h_R1...		2024-12-20 03:37:07
>> dealing withE5_0h_R2...		2024-12-20 03:37:07
>> dealing withE5_4h_R1...		2024-12-20 03:37:07
>> dealing withE5_4h_R2...		2024-12-20 03:37:07
>> dealing withE5_8h_R1...		2024-12-20 03:37:07
>> dealing withE5_8h_R2...		2024-12-20 03:37:07
>> dealing withE5_16h_R1...		2024-12-20 03:37:07
>> dealing withE5_16h_R2...		2024-12-20 03:37:07
>> dealing withE5_24h_R1...		2024-12-20 03:37:08
>> dealing withE5_24h_R2...		2024-12-20 03:37:08
>> dealing withE5_48h_R1...		2024-12-20 03:37:08
>> dealing withE5_48h_R2...		2024-12-20 03:37:08
>> dealing withE5_48h_R3...		2024-12-20 03:37:08
>> dealing withE5_72h_R1...		2024-12-20 03:37:08
>> dealing withE5_72h_R2...		2024-12-20 03:37:08
>> dealing withE5_72h_R3...		2024-12-20 03:37:08
>> merging all info together...		2024-12-20 03:37:08
>> done		2024-12-20 03:37:09
>> preparing gene features information...		2024-12-20 03:37:09
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:37:10
>> calculating p-value for each TF, which may be time consuming...		2024-12-20 03:37:10
>> merging all info together...		2024-12-20 03:37:11
>> done		2024-12-20 03:37:11
>> dealing with TF_GR_database...		2024-12-20 03:37:11
>> calculating coef and converting into z-score using INT...		2024-12-20 03:37:11
>> dealing with E5_0h_R1...		2024-12-20 03:37:11
>> dealing with E5_0h_R2...		2024-12-20 03:37:12
>> dealing with E5_4h_R1...		2024-12-20 03:37:12
>> dealing with E5_4h_R2...		2024-12-20 03:37:12
>> dealing with E5_8h_R1...		2024-12-20 03:37:12
>> dealing with E5_8h_R2...		2024-12-20 03:37:12
>> dealing with E5_16h_R1...		2024-12-20 03:37:13
>> dealing with E5_16h_R2...		2024-12-20 03:37:13
>> dealing with E5_24h_R1...		2024-12-20 03:37:13
>> dealing with E5_24h_R2...		2024-12-20 03:37:13
>> dealing with E5_48h_R1...		2024-12-20 03:37:13
>> dealing with E5_48h_R2...		2024-12-20 03:37:13
>> dealing with E5_48h_R3...		2024-12-20 03:37:14
>> dealing with E5_72h_R1...		2024-12-20 03:37:14
>> dealing with E5_72h_R2...		2024-12-20 03:37:14
>> dealing with E5_72h_R3...		2024-12-20 03:37:14
>> merging all info together...		2024-12-20 03:37:14
>> done		2024-12-20 03:37:15
>> checking seqlevels match...		2024-12-20 03:37:15
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2024-12-20 03:37:15
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:37:17
>> finding overlap peak in gene scan region...		2024-12-20 03:37:17
>> dealing with left peak not your gene scan region...		2024-12-20 03:37:17
>> merging two set peaks...		2024-12-20 03:37:17
>> calculating distance and dealing with gene strand...		2024-12-20 03:37:17
>> merging all info together ...		2024-12-20 03:37:17
>> done		2024-12-20 03:37:17
>> calculating peakCenter to TSS using peak-gene pair...		2024-12-20 03:37:17
>> calculating RP using centerToTSS and TF hit		2024-12-20 03:37:19
>> merging all info together		2024-12-20 03:37:19
>> done		2024-12-20 03:37:19
>> checking seqlevels match...		2024-12-20 03:37:20
>> your peak_GR seqlevel:5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2024-12-20 03:37:20
>> your peak_GR seqlevel:Chr5 Chr6...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
>> checking seqlevels match...		2024-12-20 03:37:26
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2024-12-20 03:37:26
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2024-12-20 03:37:26
>> finding nearest gene and calculating distance...		2024-12-20 03:37:28
>> dealing with gene strand ...		2024-12-20 03:37:28
>> merging all info together ...		2024-12-20 03:37:28
>> done		2024-12-20 03:37:28
>> checking seqlevels match...		2024-12-20 03:37:28
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2024-12-20 03:37:28
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2024-12-20 03:37:28
>> finding nearest gene and calculating distance...		2024-12-20 03:37:30
>> dealing with gene strand ...		2024-12-20 03:37:30
>> merging all info together ...		2024-12-20 03:37:30
>> done		2024-12-20 03:37:30
>> checking seqlevels match...		2024-12-20 03:37:32
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2024-12-20 03:37:32
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2024-12-20 03:37:32
>> finding nearest gene and calculating distance...		2024-12-20 03:37:34
>> dealing with gene strand ...		2024-12-20 03:37:35
>> merging all info together ...		2024-12-20 03:37:35
>> done		2024-12-20 03:37:35
>> checking seqlevels match...		2024-12-20 03:37:36
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2024-12-20 03:37:36
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2024-12-20 03:37:37
>> finding nearest gene and calculating distance...		2024-12-20 03:37:38
>> dealing with gene strand ...		2024-12-20 03:37:38
>> merging all info together ...		2024-12-20 03:37:38
>> done		2024-12-20 03:37:38
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2024-12-20 03:37:40
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2024-12-20 03:37:40
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotating Peak using nearest gene mode begins
>> preparing gene features information...		2024-12-20 03:37:40
>> finding nearest gene and calculating distance...		2024-12-20 03:37:42
>> dealing with gene strand ...		2024-12-20 03:37:42
>> merging all info together ...		2024-12-20 03:37:42
>> done		2024-12-20 03:37:42
It seems that there 1 genes have not been annotated by nearestGene mode
>> checking seqlevels match...		2024-12-20 03:37:44
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> checking seqlevels match...		2024-12-20 03:37:47
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:37:48
>> checking seqlevels match...		2024-12-20 03:37:50
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:37:51
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2024-12-20 03:37:54
>> merging all info together...		2024-12-20 03:37:55
>> done		2024-12-20 03:37:55
>> checking seqlevels match...		2024-12-20 03:37:55
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> using scanPromoter parameter to scan promoter for each gene...		2024-12-20 03:37:55
>> checking seqlevels match...		2024-12-20 03:37:55
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:37:56
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2024-12-20 03:37:57
>> checking seqlevels match...		2024-12-20 03:37:57
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:37:59
>> calculating cor and pvalue, which may be time consuming...		2024-12-20 03:37:59
>> merging all info together...		2024-12-20 03:38:00
>> done		2024-12-20 03:38:00
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2024-12-20 03:38:00
>> merging all info together...		2024-12-20 03:38:00
>> done		2024-12-20 03:38:00
>> checking seqlevels match...		2024-12-20 03:38:00
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
------------
annotatePeak using geneScan mode begins
>> preparing gene features information and scan region...		2024-12-20 03:38:01
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:38:02
>> finding overlap peak in gene scan region...		2024-12-20 03:38:02
>> dealing with left peak not your gene scan region...		2024-12-20 03:38:02
>> merging two set peaks...		2024-12-20 03:38:02
>> calculating distance and dealing with gene strand...		2024-12-20 03:38:02
>> merging all info together ...		2024-12-20 03:38:02
>> done		2024-12-20 03:38:03
Good, your two matrix colnames matchs
>> calculating cor and pvalue, which may be time consuming...		2024-12-20 03:38:05
>> merging all info together...		2024-12-20 03:38:05
>> done		2024-12-20 03:38:06
>> checking seqlevels match...		2024-12-20 03:38:06
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> using scanPromoter parameter to scan promoter for each gene...		2024-12-20 03:38:06
>> checking seqlevels match...		2024-12-20 03:38:06
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:38:07
>> there are 85 gene have scaned promoter
>> using scanEnhancer parameter to scan Enhancer for each gene...		2024-12-20 03:38:08
>> checking seqlevels match...		2024-12-20 03:38:08
>> your peak_GR seqlevel:Chr5...
>> your Txdb seqlevel:Chr1 Chr2 Chr3 Chr4 Chr5 ChrM ChrC...
Good, your Chrs in peak_GR is all in Txdb
>> some scan range may cross Chr bound, trimming...		2024-12-20 03:38:10
>> calculating cor and pvalue, which may be time consuming...		2024-12-20 03:38:10
>> merging all info together...		2024-12-20 03:38:10
>> done		2024-12-20 03:38:11
Joining with `by = join_by(feature_id)`
Joining with `by = join_by(feature_id)`
`geom_smooth()` using formula = 'y ~ x'
Joining with `by = join_by(feature_id)`
Joining with `by = join_by(feature_id)`
`geom_smooth()` using formula = 'y ~ x'
[ FAIL 0 | WARN 0 | SKIP 0 | PASS 65 ]
> 
> proc.time()
   user  system elapsed 
130.672   4.096 139.791 

Example timings

FindIT2.Rcheck/FindIT2-Ex.timings

nameusersystemelapsed
TF_target_database0.0000.0020.002
calcRP_TFHit6.6090.3127.529
calcRP_coverage5.7930.5627.175
calcRP_region10.931 0.17811.670
enhancerPromoterCor5.4300.0895.959
findIT_MARA0.9810.0191.078
findIT_TFHit2.8090.0512.922
findIT_TTPair0.1490.0090.167
findIT_enrichFisher0.3490.0080.378
findIT_enrichWilcox0.3700.0080.391
findIT_regionRP11.780 0.16012.262
getAssocPairNumber2.3040.0372.361
integrate_ChIP_RNA4.0920.0684.218
integrate_replicates0.0040.0020.006
jaccard_findIT_TTpair0.2350.0150.277
jaccard_findIT_enrichFisher0.4320.0080.448
loadPeakFile0.1310.0030.139
mm_geneBound2.4030.0452.559
mm_geneScan2.4590.0422.552
mm_nearestGene2.1060.0332.157
peakGeneCor6.5740.2457.165
plot_annoDistance2.9750.0523.104
plot_peakGeneAlias_summary2.7160.0492.840
plot_peakGeneCor6.8300.0807.011
test_geneSet0.0000.0010.002